Duttaroy A, McCarron M, Sitaraman K, Doughty G, Chovnick A
Department of Molecular and Cell Biology, University of Connecticut, Storrs 06268.
Genetics. 1990 Feb;124(2):317-29. doi: 10.1093/genetics/124.2.317.
P element dysgenesis associated male recombination in Drosophila was examined with a selective system focused upon 5% of the standard female genetic map divided into eight recombination segments. We found no correspondence between P element mobilization events and recombination in males in the intervals monitored. We defined two adjacent short genetic and molecular regions, one devoid of male recombination and the other acting as a "hot spot" for exchange in the absence of supporting P element insertion and excision activity. These data suggest that, even in the presence of mobilizing P elements, transposase may be active at non-P element sites, and that the genome may harbor sequences ranging from highly responsive to completely unresponsive to transposase action. A viewpoint is presented wherein P elements, with sequences that bind transposase, serve to focus the recombination action of transposase to encompass a region of DNA radiating outward from the initial binding site. We suggest that this region is measured in terms of chromosomal segments rather than limited to P element sequences.
利用一个针对标准雌性遗传图谱5%的选择性系统,该系统被划分为八个重组区段,对果蝇中与P因子发育不全相关的雄性重组进行了研究。在监测的区间内,我们未发现P因子移动事件与雄性重组之间存在对应关系。我们定义了两个相邻的短遗传和分子区域,一个没有雄性重组,另一个在没有支持性P因子插入和切除活性的情况下作为交换的“热点”。这些数据表明,即使存在移动的P因子,转座酶可能在非P因子位点具有活性,并且基因组可能含有对转座酶作用从高度敏感到完全无反应的各种序列。提出了一种观点,其中具有结合转座酶序列的P因子,用于聚焦转座酶的重组作用,以涵盖从初始结合位点向外辐射的DNA区域。我们认为这个区域是以染色体区段来衡量的,而不限于P因子序列。